3814d8eec23ed1c9f539f669383099eb605dbbcd
mspeir
  Sat Sep 26 18:18:00 2026 -0700
Regulation FAQ: link hgCustom as well as the custom track help, refs #24610

diff --git src/hg/htdocs/FAQ/FAQregulation.html src/hg/htdocs/FAQ/FAQregulation.html
index debed8a8caa..8e06956e0c6 100755
--- src/hg/htdocs/FAQ/FAQregulation.html
+++ src/hg/htdocs/FAQ/FAQregulation.html
@@ -120,33 +120,34 @@
 experiments that were available when it was built, so if your factor is absent from ReMap there
 may be no public ChIP-seq for it in that organism. The
 <a href="https://remap.univ-amu.fr/" target="_blank">ReMap website</a> lets you search by target
 and download the peaks per factor, and that is the quickest way to check.</p>
 <p>
 If the experiment exists but is newer than our tracks, or was done in a cell type we do not
 carry, you will need to load the data yourself as a custom track. The usual sources are:</p>
 <ul>
   <li>
   The <a href="https://www.encodeproject.org/" target="_blank">ENCODE portal</a>, for anything
   produced by ENCODE. This is the easiest case, because the portal will send the data
   straight to our browser for you. See the <a href="#encodePortal">next question</a>.</li>
   <li>
   <a href="https://www.ncbi.nlm.nih.gov/geo/" target="_blank">GEO</a>, for data submitted
   alongside a publication. Many GEO submissions include processed peak files as supplementary
-  material, usually BED or narrowPeak, which you can load as a
-  <a href="/goldenPath/help/customTrack.html">custom track</a> after checking that the
-  coordinates match the assembly you are using.</li>
+  material, usually BED or narrowPeak, which you can
+  <a href="/goldenPath/help/customTrack.html">load as a custom track</a> at
+  <a href="../cgi-bin/hgCustom">Add Custom Tracks</a>, after checking that the coordinates
+  match the assembly you are using.</li>
   <li>
   <a href="https://www.ncbi.nlm.nih.gov/sra" target="_blank">SRA</a>, for raw sequencing reads.
   The Browser cannot display SRA data. Raw reads have to be aligned and peak-called before there
   is anything to show, which is a job for a sequence analysis pipeline rather than for us.</li>
 </ul>
 
 <a name="encodePortal"></a>
 <h6>How do I display ENCODE data that is not already a track?</h6>
 <p>
 You do not need to download anything or write a custom track by hand. The ENCODE portal will
 open its data in the Genome Browser for you.</p>
 <ol>
   <li>
   Search the <a href="https://www.encodeproject.org/search/?type=Experiment"
   target="_blank">ENCODE portal</a> for what you want, narrowing the results with the filters